A copper(ii)–thioamide combination as a robust heterogeneous catalytic system for green synthesis of 1,4-disubstituted-1,2,3-triazoles under click conditions-Reference-Cited by-同舟云学术

A copper(ii)–thioamide combination as a robust heterogeneous catalytic system for green synthesis of 1,4-disubstituted-1,2,3-triazoles under click conditions

Published:2015 Issue:95 Volume:5 Page:78038-78046
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Mirjafary Zohreh¹²³⁴⁵,Ahmadi Leila⁶⁷⁴⁵,Moradi Masomeh⁶⁷⁴⁵,Saeidian Hamid⁶⁷⁴⁵

Affiliation:

1. Department of Chemistry

2. Tehran Science and Research Branch

3. Islamic Azad University

4. Tehran

5. Iran

6. Department of Science

7. Payame Noor University (PNU)

Abstract

One-pot synthesis of 1,4-disubstituted-1,2,3-triazoles 3 using copper(ii)–thioamide combination was reported.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA16581D

Reference38 articles.

1. Click Chemistry for Drug Development and Diverse Chemical–Biology Applications

2. Tricks with clicks: modification of peptidomimetic oligomers via copper-catalyzed azide-alkyne [3 + 2] cycloaddition

3. Cu(I)-Catalyzed Huisgen Azide−Alkyne 1,3-Dipolar Cycloaddition Reaction in Nucleoside, Nucleotide, and Oligonucleotide Chemistry

4. Efficiency and Fidelity in a Click-Chemistry Route to Triazole Dendrimers by the Copper(I)-Catalyzed Ligation of Azides and Alkynes

5. Novel nucleobase-simplified cyclic ADP-ribose analogue: A concise synthesis and Ca2+-mobilizing activity in T-lymphocytes

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